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- Tasks: Ensure regulatory compliance and manage license submissions across UK, EU, and global markets.
- Company: Join a leading pharmaceutical organization dedicated to patient safety and compliance excellence.
- Benefits: Enjoy remote work flexibility with occasional travel and a dynamic team environment.
- Why this job: Make a real impact in regulatory affairs while working with top professionals in the industry.
- Qualifications: Requires a Life Science degree and 3+ years of regulatory affairs experience.
- Other info: Interviews in November, with a start date planned for January.
The predicted salary is between 36000 - 60000 £ per year.
Are you ready to take the next step in your regulatory affairs career? We are partnering with a leading pharmaceutical organisation to find a skilled Regulatory Affairs Specialist who is passionate about ensuring compliance and safeguarding patient safety. This exciting role offers the opportunity to work across UK, EU, and global markets. Key Responsibilities Regulatory Compliance : Ensure adherence to regulatory requirements across UK, EU, and global regions, managing license submissions, variations, renewals, and inspections. Interaction with Regulatory Authorities: Acting as a key contact with regulatory bodies for inspections, audits or clarifications regarding services Stakeholder Support : Provide strategic guidance on regulatory requirements to senior management, liaise with regulatory authorities, and foster strong relationships with stakeholders. Licensing and Accreditation: Managing regulatory requirements for licenses, such as WDA and GDP compliance, ensuring the safe handling, storage and transport of medicines Qualifications and Skills A Life Science degree or equivalent professional qualification. Strong interpersonal and communication skills (written, oral, and presentational). Proven ability to influence stakeholders and drive service improvements. 3+ Years experience in within regulatory affairs Experience in regulatory strategy for importing and exporting in EU countries Strong problem-solving and analytical skills with a track record of delivering results in GDP environments. Experience leading change management projects and implementing business improvements. What We Offer This role is primarily remote, with occasional travel to London and very infrequent trips to the Netherlands. Join a forward-thinking team in a dynamic organisation committed to excellence in pharmaceutical compliance. Interviews will take place in November, with a planned start date in January. For any questions, feel free to reach out directly.
Regulatory Specialist employer: William Parker Group
Contact Detail:
William Parker Group Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Regulatory Specialist
✨Tip Number 1
Familiarize yourself with the specific regulatory frameworks in the UK, EU, and global markets. Understanding the nuances of these regulations will not only boost your confidence during discussions but also demonstrate your commitment to compliance.
✨Tip Number 2
Network with professionals in the regulatory affairs field. Attend industry conferences or webinars where you can meet key players and learn about current trends. This can help you gain insights and potentially get referrals for the position.
✨Tip Number 3
Prepare to discuss your experience with license submissions and regulatory inspections in detail. Be ready to share specific examples of how you've navigated challenges in these areas, as this will showcase your expertise and problem-solving skills.
✨Tip Number 4
Research the pharmaceutical organization you're applying to. Understand their products, market presence, and any recent news. This knowledge will help you tailor your conversations and show that you're genuinely interested in contributing to their success.
We think you need these skills to ace Regulatory Specialist
Some tips for your application 🫡
Understand the Role: Make sure to thoroughly read the job description for the Regulatory Specialist position. Highlight key responsibilities and qualifications that resonate with your experience and skills.
Tailor Your CV: Customize your CV to reflect your relevant experience in regulatory affairs, particularly focusing on compliance, stakeholder interaction, and licensing. Use specific examples that demonstrate your achievements in these areas.
Craft a Compelling Cover Letter: Write a cover letter that showcases your passion for regulatory affairs and patient safety. Mention your experience with UK, EU, and global markets, and how you can contribute to the organization’s goals.
Highlight Soft Skills: Emphasize your strong interpersonal and communication skills in both your CV and cover letter. Provide examples of how you've influenced stakeholders and driven service improvements in previous roles.
How to prepare for a job interview at William Parker Group
✨Understand Regulatory Compliance
Make sure you have a solid grasp of the regulatory requirements across UK, EU, and global markets. Be prepared to discuss your experience with license submissions, variations, renewals, and inspections, as this will demonstrate your expertise in the field.
✨Showcase Your Communication Skills
Since strong interpersonal and communication skills are crucial for this role, practice articulating your thoughts clearly. Prepare examples of how you've effectively communicated with regulatory authorities or stakeholders in the past.
✨Highlight Your Problem-Solving Abilities
Be ready to share specific instances where you've tackled challenges in regulatory affairs. Discuss your analytical skills and how you've delivered results in GDP environments, as this will showcase your capability to handle complex situations.
✨Demonstrate Stakeholder Engagement
Prepare to discuss how you've influenced stakeholders and driven service improvements in previous roles. Highlight any experience you have in providing strategic guidance to senior management, as this will be key to your success in the position.
